Canonical Allele Identifier: CA2658238127

Gene: OTOF

Linked Data

• gnomAD v4: 2-26480663-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480664_26480665dup , CM000664.2:g.26480664_26480665dup	GRCh38
NC_000002.11:g.26703532_26703533dup , CM000664.1:g.26703532_26703533dup	GRCh37
NC_000002.10:g.26557036_26557037dup	NCBI36
NG_009937.1:g.83034_83035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1803+121_1803+122dup MANE Select	ENSP00000272371.2:n.1803+121_1803+122dup
ENST00000272371.6:c.1803+121_1803+122dup	ENSP00000272371.2:n.1803+121_1803+122dup
ENST00000403946.7:c.1803+121_1803+122dup	ENSP00000385255.3:n.1803+121_1803+122dup
NM_001287489.1:c.1803+121_1803+122dup	NP_001274418.1:n.1803+121_1803+122dup
NM_194248.2:c.1803+121_1803+122dup	NP_919224.1:n.1803+121_1803+122dup
XM_005264644.2:c.1848+121_1848+122dup	XP_005264701.1:n.1848+121_1848+122dup
XM_011533185.1:c.1848+121_1848+122dup	XP_011531487.1:n.1848+121_1848+122dup
XM_017005338.1:c.1803+121_1803+122dup	XP_016860827.1:n.1803+121_1803+122dup
NM_001287489.2:c.1803+121_1803+122dup	NP_001274418.1:n.1803+121_1803+122dup
NM_194248.3:c.1803+121_1803+122dup MANE Select	NP_919224.1:n.1803+121_1803+122dup